Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imatinib | HCID 5291 | — |
| Reactant | Benzenesulfonic Acid | HCID 7371 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Imatinib | HCID 5291 | — |
| Product | Benzenesulfonate | HCID 91526 | — |
Reaction Steps
4-[(4-Methyl-1-piperazinyl)methyl]-N-[4-methyl-3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]phenyl]-benzamide (4.94 g, 10 mmol) is added to a solution of benzenesulphonic acid (Fluka, Buchs, Switzerland; 1.61 g, 10 mmol) in hot toluene (40 mL). The solution is evaporated to dryness under reduced pressure and the resulting residue is re-crystallized from ethanol-ethylacetate. The product is filtered-off and dried to afford 4-[(4-methyl-1-piperazinyl)methyl]-N-[4-methyl-3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]phenyl]-benzamide, benzenesulphonate as a pale-yellow crystalline solid, having the following analytical properties: Analysis found: C, 64.19; H, 5.68; N, 14.93; S, 4.87%; H2O, 0.34%. Calculated for C35H37N7O4S-0.12 H2O: C, 64.28; H, 5.74; N, 14.99; S, 4.90%; H2O, 0.33%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08513256B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-62bb0c24969843e3bc6c944bd45fa369 |
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| Source note | uspto-grants-2013_08 |
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